Maldonado-Rodriguez R, Espinosa-Lara M, Beattie K L
Verna and Marrs McLean Department of Biochemistry, Baylor College of Medicine, Houston, TX 77030.
Mutat Res. 1991 Dec;251(2):217-26. doi: 10.1016/0027-5107(91)90076-z.
Genetic and electrophoretic assays of misincorporation were used to assess the effect of DNA sequence on mutagenesis arising from in vitro DNA synthesis within the lacI gene of Escherichia coli. The viral strand of a derivative of phage M13 containing the entire lacI gene was annealed with a series of synthetic oligonucleotides complementary to the N-terminal region of the lacI gene. Each primer-template was incubated with E. coli DNA polymerase I (Klenow fragment) under conditions favoring misincorporation, wherein one of the 4 dNTPs was lacking ('minus' reaction) or present at very low concentration ('micro' reaction). The extent of elongation of each primer was assessed by gel electrophoresis, and lacI mutants arising during the misincorporation reactions were detected by a transfection assay in which i- base substitutions within the in vitro synthesized strand were selectively recovered by the use of uracil-containing templates. Direct dideoxy sequencing of the '-A' reaction products and sequence analysis of i- mutant progeny revealed a vast predominance of single and non-tandem multiple base transitions. The addition of small quantities of dATP to a '-A' reaction increased the mutation yield and broadened the distribution of base substitutions along the template. We detected a general bias towards increased base substitution at template positions flanked by G.C base pairs or 5'-pyrimidine, 3'-purine nearest neighbors, although considerable site-to-site variation in the occurrence of base substitutions was seen, even within identical nearest neighbor contexts.
利用错配掺入的遗传和电泳分析方法,评估DNA序列对大肠杆菌lacI基因体外DNA合成引发的诱变作用。将含有完整lacI基因的噬菌体M13衍生物的病毒链与一系列与lacI基因N端区域互补的合成寡核苷酸退火。在有利于错配掺入的条件下,将每个引物 - 模板与大肠杆菌DNA聚合酶I(Klenow片段)一起孵育,其中4种dNTP之一缺失(“减”反应)或存在于非常低的浓度(“微量”反应)。通过凝胶电泳评估每个引物的延伸程度,并通过转染分析检测错配掺入反应期间产生的lacI突变体,其中通过使用含尿嘧啶的模板选择性回收体外合成链内的i - 碱基取代。对“-A”反应产物进行直接双脱氧测序以及对i - 突变后代进行序列分析,结果显示单碱基和非串联多碱基转换占主导地位。向“-A”反应中添加少量dATP可提高突变率,并拓宽沿模板的碱基取代分布。我们检测到在由G.C碱基对或5'-嘧啶、3'-嘌呤最近邻侧翼的模板位置上碱基取代增加的普遍偏向,尽管即使在相同的最近邻背景下,碱基取代的发生也存在相当大的位点间差异。